Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion type Assertion NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_head.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion description "[Werner syndrome (WS) is a progeroid syndrome caused by autosomal recessive null mutations at the WRN locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion evidence source_evidence_literature NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion SIO_000772 11186893 NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion wasDerivedFrom befree-2016 NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.
- NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_assertion wasGeneratedBy ECO_0000203 NP307697.RAHKvn4fxYQJovSQcqyM3oyuRVklcmGxDV0Zbe1VK21d8130_provenance.